SPINDLE CELL LIPOMA MASQUERADING AS MIXED PYOLARYNGOCELE : A RARE CASE REPORT

2020 ◽  
Vol VOLUME 8 (ISSUE 1) ◽  
pp. 47-51
Author(s):  
Vineet Narula
Keyword(s):  
Rare Case ◽  
Spindle Cell ◽  
Spindle Cell Lipoma ◽  
Computed Tomographic ◽  
Contrast Enhanced ◽  
Rare Case Report ◽  
Shoulder Region ◽  
Cervical Approach ◽  
Posterior Neck ◽  
Keywords Lipoma

ABSTRACT Spindle Cell Lipoma (SCL) is an uncommon benign tumor of adipose tissue that is usually super􀃶cially located in the posterior neck, back and shoulder region. We report a rare case of SCL in a 39 years old male presenting as neck swelling with c/o stridor and dysphagia. The contrast enhanced computed tomographic scan of neck showed an external and internal part of the swelling traversing through the thyrohyoid membrane suggestive of Mixed Pyolaryngocele. The tumor was excised by a trans-cervical approach but the post operative histopathology was found to be spindle cell Lipoma. We report this case due to its atypical presentation and location. Keywords: Lipoma, Spindle cell, Pyolaryngocele

Bucco-Parapharyngeal Occurrence of Pleomorphic Spindle Cell Lipoma-A Unique Entity: Case Report

2020 ◽  
Vol 44 (2) ◽  
pp. 107-111
Author(s):  
Gopikrishnan Vijayakumar ◽  
Mala Kamboj ◽  
Anjali Narwal ◽  
Anju Devi ◽  
Virendra Singh
Keyword(s):  
Rare Case ◽  
Literature Search ◽  
Benign Tumor ◽  
Spindle Cell ◽  
Parapharyngeal Space ◽  
Age Distribution ◽  
Rare Entity ◽  
Spindle Cell Lipoma ◽  
Shoulder Region ◽  
Buccal Space

Lipomas are common benign neoplasms of oral region which occur scarcely in the parapharyngeal space (PPS). The diversity observed in its histologic presentation classified it into many subtypes among which Spindle Cell Lipoma (SCL) is a rare entity. SCL is an uncommon benign tumor of adipose tissue usually located superficially in the neck, back and shoulder region but its presentation in oral and pharyngeal spaces is very rare. Exhaustive literature search for oral and pharyngeal space pleomorphic SCL till date revealed 45 cases of oral SCL with a mean age distribution of 55 years. Only one reported case of parapharyngeal occurrence of pleomorphic SCL was found. A rare case of pleomorphic variant of SCL in PPS extending into the buccal space is being presented. This case could be the first to report the multiple presentation and the youngest age of occurrence of SCL in PPS.

scholarly journals Aggressive Monophasic Sarcomatoid Carcinoma of Small Intestine - A Rare Case Report With Review of Literature

2012 ◽  
Vol 02 (01) ◽  
pp. 45-47
Author(s):  
Shetty K. Padma ◽  
Harish S. Permi ◽  
C.N. Patil ◽  
Michelle Mathias
Keyword(s):  
Small Intestine ◽  
Rare Case ◽  
Spindle Cell ◽  
Correct Diagnosis ◽  
Sarcomatoid Carcinoma ◽  
Intestinal Wall ◽  
Cell Tumor ◽  
Review Of Literature ◽  
Spindle Cells ◽  
Rare Case Report

AbstractSarcomatoid carcinoma occurring in the small intestine is very rare. They can be monophasic or biphasic. We report a rare case of monophasic Sarcomatoid carcinoma of the small intestine in a 60 year old male patient. The tumor was an ulceronodular mass involving the ileum circumferentially. The tumor infiltrated the full thickness of the intestinal wall and the serosa of an adjacent loop of ileum. Microscopically, the tumor was composed of sheets of malignant spindle cells. The carcinomatous nature of the tumor was evident only after Immunohistochemistry. The diagnosis of sarcomatoid carcinoma should be considered in the differential diagnosis of malignant spindle cell tumor of small intestine and immunohistochemical stains are required for the correct diagnosis.

scholarly journals A Rare Case of Spindle Cell Lipoma of Nose

2012 ◽  
Vol 4 (2) ◽  
pp. 110 ◽  
Author(s):  
Deepalakshmi Tanthry ◽  
PP Devan ◽  
KavithaAshok Kumar ◽  
Rukma Bhandary
Keyword(s):  
Rare Case ◽  
Spindle Cell ◽  
Spindle Cell Lipoma

scholarly journals Paratesticular Embryonal Rhabdomyosarcoma with Lung Metastasis – A Rare Case Report

2020 ◽  
Vol 7 (11) ◽  
pp. C164-168
Author(s):  
Anusha Ganapathi ◽  
Thanka J ◽  
Lawrence D'Cruze ◽  
Barathi G ◽  
Natarajan K ◽  
...  
Keyword(s):  
Lung Metastasis ◽  
Spermatic Cord ◽  
Rare Case ◽  
Spindle Cell ◽  
Malignant Tumors ◽  
Embryonal Rhabdomyosarcoma ◽  
Cell Component ◽  
Testicular Tumors ◽  
Spindle Cell Component ◽  
Rare Case Report

Paratesticular rhabdomyosarcomas (RMS) are very rare malignant tumors arising from the mesenchymal tissues of tunica, epididymis or spermatic cord. They present as painless hard masses in inguinoscrotal region, and large tumors can be mistaken for testicular tumors. They can spread to retroperitoneal lymph nodes or hematogenously metastasize to lung, bones and bone marrow. Here, we report a case of Embryonal RMS with spindle cell component presenting with painless scrotal mass and lung metastasis at initial diagnosis.

scholarly journals Pleomorphic lipoma: A rare entity

2021 ◽  
Vol 8 (4) ◽  
pp. 515-517
Author(s):  
Goutami Das Nayak ◽  
Shushruta Mohanty ◽  
Meenakshi Mohapatro
Keyword(s):  
Spindle Cell ◽  
Histopathological Diagnosis ◽  
Spindle Cell Lipoma ◽  
Soft Tissue Tumours ◽  
Pleomorphic Lipoma ◽  
Atypical Cells ◽  
Posterior Neck ◽  
Subcutaneous Mass ◽  
Slow Growing ◽  
Malignant Soft Tissue

Pleomorphic lipoma is a rare neoplasm that is considered as a variant of spindle cell lipoma. It predominantly occurs in the dermis or subcutis of the posterior neck, upper back, and shoulders. Pleomorphic lipoma may clinically present as a slow-growing and well-circumscribed subcutaneous mass. Though it is a benign tumour it may contain atypical cells for which it may mimick sarcoma or other malignant soft tissue tumours. So histopathological diagnosis is vital for preventing unnecessary surgery. Here we report a case of a pleomorphic lipoma on upper back in a 55yr old patient.

scholarly journals Pulmonary Spindle Cell Carcinoma: A Rare Case Report

Cureus ◽  
2019 ◽  
Author(s):  
Salman Khan ◽  
Binita Dahal ◽  
Faraz Siddiqui ◽  
Kim J Norville ◽  
Apurwa Karki
Keyword(s):  
Case Report ◽  
Cell Carcinoma ◽  
Rare Case ◽  
Spindle Cell ◽  
Spindle Cell Carcinoma ◽  
Rare Case Report
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